TW200930382A - LNA antagonists targeting the androgen receptor - Google Patents
LNA antagonists targeting the androgen receptor Download PDFInfo
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- TW200930382A TW200930382A TW097145706A TW97145706A TW200930382A TW 200930382 A TW200930382 A TW 200930382A TW 097145706 A TW097145706 A TW 097145706A TW 97145706 A TW97145706 A TW 97145706A TW 200930382 A TW200930382 A TW 200930382A
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EP3415625A1 (en) | 2002-02-01 | 2018-12-19 | Life Technologies Corporation | Double-stranded oligonucleotides |
US20060009409A1 (en) | 2002-02-01 | 2006-01-12 | Woolf Tod M | Double-stranded oligonucleotides |
EP1572902B1 (en) | 2002-02-01 | 2014-06-11 | Life Technologies Corporation | HIGH POTENCY siRNAS FOR REDUCING THE EXPRESSION OF TARGET GENES |
JP5723154B2 (ja) * | 2007-09-19 | 2015-05-27 | アプライド バイオシステムズ リミテッド ライアビリティー カンパニー | RNAiにおけるオフターゲット表現型の影響を減少させるためのSiRNA配列非依存性修飾フォーマットおよびその安定化型 |
US8450290B2 (en) * | 2007-11-26 | 2013-05-28 | Enzon Pharmaceuticals, Inc. | Methods for treating androgen receptor dependent disorders including cancers |
EP3210611B1 (en) | 2010-03-12 | 2019-08-21 | The Brigham and Women's Hospital, Inc. | Methods of treating vascular inflammatory disorders |
US20130253035A1 (en) * | 2010-08-16 | 2013-09-26 | Duke University | Camkk-beta as a target for treating cancer |
CN103517990A (zh) | 2010-10-07 | 2014-01-15 | 通用医疗公司 | 癌症生物标志物 |
AU2011326034B2 (en) | 2010-11-12 | 2016-02-04 | Roche Innovation Center Copenhagen A/S | Compositions and methods for treating androgen receptor dependent disorders including cancers |
EP2638163B1 (en) | 2010-11-12 | 2017-05-17 | The General Hospital Corporation | Polycomb-associated non-coding rnas |
US9045749B2 (en) | 2011-01-14 | 2015-06-02 | The General Hospital Corporation | Methods targeting miR-128 for regulating cholesterol/lipid metabolism |
ES2622112T3 (es) | 2011-05-02 | 2017-07-05 | Stichting Vumc | Protección contra la disfunción de la barrera endotelial a través de la inhibición del gen relacionado con la tirosina quinasa Abl (ARG) |
JP6234370B2 (ja) | 2011-10-11 | 2017-11-22 | ザ ブリガム アンド ウィメンズ ホスピタル インコーポレイテッドThe Brigham and Women’s Hospital, Inc. | 神経変性障害におけるマイクロrna |
WO2013184209A1 (en) | 2012-06-04 | 2013-12-12 | Ludwig Institute For Cancer Research Ltd. | Mif for use in methods of treating subjects with a neurodegenerative disorder |
NZ742581A (en) * | 2012-07-27 | 2020-02-28 | Aragon Pharmaceuticals Inc | Methods and compositions for determining resistance to androgen receptor therapy |
WO2014048441A1 (en) | 2012-09-26 | 2014-04-03 | Mirrx Therapeutics | Oligomers with improved off-target profile |
US9175291B2 (en) | 2012-10-11 | 2015-11-03 | Isis Pharmaceuticals Inc. | Modulation of androgen receptor expression |
US9523094B2 (en) | 2012-10-11 | 2016-12-20 | Ionis Pharmaceuticals, Inc. | Methods of treating kennedy's disease |
RU2653438C2 (ru) | 2012-11-15 | 2018-05-08 | Рош Инновейшен Сентер Копенгаген А/С | Конъюгаты олигонуклеотидов |
SG11201505387PA (en) * | 2013-01-30 | 2015-08-28 | Hoffmann La Roche | Lna oligonucleotide carbohydrate conjugates |
EP2774997A1 (en) * | 2013-03-05 | 2014-09-10 | Bayer Pharma Aktiengesellschaft | Detection of Androgen Receptor (AR) mutations in circulating tumor DNA from plasma samples of castration-resistant prostate cancer patients using locked nucleic acid-clamp PCR |
WO2014171826A1 (en) | 2013-04-17 | 2014-10-23 | Stichting Vu-Vumc | Treatment of cognitive impairment in depressive disorders |
WO2014179446A2 (en) | 2013-05-01 | 2014-11-06 | Regulus Therapeutics Inc. | Microrna compounds and methods for modulating mir-122 |
TWI680767B (zh) | 2013-05-01 | 2020-01-01 | 美商雷格勒斯治療公司 | 用於增強的細胞攝取之化合物及方法 |
BR112016003127A2 (pt) * | 2013-08-16 | 2017-10-17 | Rana Therapeutics Inc | composições e métodos para modular rna |
WO2015200697A1 (en) | 2014-06-25 | 2015-12-30 | The General Hospital Corporation | Targeting human satellite ii (hsatii) |
EP3185910A4 (en) | 2014-08-29 | 2018-01-10 | Children's Medical Center Corporation | Methods and compositions for the treatment of cancer |
WO2016114655A1 (en) | 2015-01-12 | 2016-07-21 | Ry Pharma B.V. | Treating neuromuscular or neurologic disease through reducing gabaergic and/or glycinergic inhibitory neurotransmitter overstimulation |
EP3256591A4 (en) | 2015-02-13 | 2018-08-08 | Translate Bio Ma, Inc. | Hybrid oligonucleotides and uses thereof |
EP3283502A4 (en) | 2015-04-07 | 2019-04-03 | The General Hospital Corporation | METHOD FOR REACTIVATING GENES ON THE INACTIVE X-CHROMOSOME |
AU2016282986A1 (en) | 2015-06-26 | 2018-02-01 | Beth Israel Deaconess Medical Center, Inc. | Cancer therapy targeting tetraspanin 33 (tspan33) in myeloid derived suppressor cells |
WO2017065602A1 (en) | 2015-10-13 | 2017-04-20 | Ry Pharma B.V. | Treating neuromuscular or neurologic disease through reducing gabaergic and/or glycinergic inhibitory neurotransmitter overstimulation |
WO2017066796A2 (en) | 2015-10-16 | 2017-04-20 | The Children's Medical Center Corporation | Modulators of telomere disease |
WO2017066712A2 (en) | 2015-10-16 | 2017-04-20 | The Children's Medical Center Corporation | Modulators of telomere disease |
AU2016344384A1 (en) | 2015-10-26 | 2018-05-17 | Translate Bio Ma, Inc. | Nanoparticle formulations for delivery of nucleic acid complexes |
US11001622B2 (en) | 2015-11-19 | 2021-05-11 | The Brigham And Women's Hospital, Inc. | Method of treating autoimmune disease with lymphocyte antigen CD5-like (CD5L) protein |
ES2999146T3 (en) | 2016-02-25 | 2025-02-24 | Brigham & Womens Hospital Inc | Treatment methods for fibrosis targeting smoc2 |
AU2017237643B2 (en) | 2016-03-24 | 2023-06-22 | Academisch Ziekenhuis Leiden H.O.D.N. Lumc | Methods for transfecting plants and for reducing random integration events |
US11041152B2 (en) * | 2016-04-14 | 2021-06-22 | E-Na Biotec Inc. | MicroRNA-143 derivative |
CN110072879B (zh) * | 2016-08-08 | 2023-03-10 | 奥利通公司 | 雄激素受体反义寡核苷酸 |
EP3532638A4 (en) | 2016-10-31 | 2020-07-29 | University of Massachusetts | TARGETING MICROARN-101-3 P IN CARCINOTHERAPY |
WO2018093919A1 (en) * | 2016-11-15 | 2018-05-24 | City Of Hope | Methods for intracellular delivery and enhanced gene targeting |
WO2018111099A1 (en) | 2016-12-12 | 2018-06-21 | Stichting Vumc | Biomarkers and treatments for cerebral amyloid angiopathy (caa) |
WO2018195486A1 (en) | 2017-04-21 | 2018-10-25 | The Broad Institute, Inc. | Targeted delivery to beta cells |
US11821003B2 (en) | 2017-08-14 | 2023-11-21 | Sanford Burnham Prebys Medical Discovery Institute | Cardiogenic mesoderm formation regulators |
WO2019089216A1 (en) | 2017-11-01 | 2019-05-09 | Dana-Farber Cancer Institute, Inc. | Methods of treating cancers |
EP3502259A1 (en) | 2017-12-19 | 2019-06-26 | Universiteit Leiden | A combinational strategy for reducing random integration events when transfecting plants |
CA3099698A1 (en) | 2018-05-08 | 2019-11-14 | Charles R. ALLERSON | Galnac conjugated modified oligonucleotide as mir-122 inhibitor having hcv antiviral activity with reduced hyperbilirubinemia side-effect |
CA3110661A1 (en) | 2018-08-29 | 2020-03-05 | University Of Massachusetts | Inhibition of protein kinases to treat friedreich ataxia |
WO2020067887A1 (en) | 2018-09-24 | 2020-04-02 | Erasmus University Medical Center Rotterdam | Specific inhibition of janus kinase 3 (jak3) for modulating anti-tumor immune responses |
GB201817990D0 (en) * | 2018-11-02 | 2018-12-19 | Univ Of Essex Enterprise Limited | Enzymatic nucleic acid molecules |
KR102473989B1 (ko) | 2018-11-28 | 2022-12-07 | (주)바이오니아 | 안드로젠 수용체 특이적 서열을 포함하는 이중나선 올리고뉴클레오티드 구조체, 및 이를 포함하는 탈모 예방 및 발모용 조성물 |
WO2020148400A1 (en) * | 2019-01-16 | 2020-07-23 | Stichting Katholieke Universiteit | Antisense oligonucleotides for use in the treatment of crpc |
WO2020171889A1 (en) | 2019-02-19 | 2020-08-27 | University Of Rochester | Blocking lipid accumulation or inflammation in thyroid eye disease |
CN119979543B (zh) * | 2025-04-14 | 2025-07-22 | 羿美诚健(上海)生物医药有限公司 | 靶向雄激素受体的小核酸及其药物组合物和用途 |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4962029A (en) | 1987-10-02 | 1990-10-09 | Cetus Corporation | Covalent oligonucleotide-horseradish peroxidase conjugate |
US4914210A (en) | 1987-10-02 | 1990-04-03 | Cetus Corporation | Oligonucleotide functionalizing reagents |
US6733776B1 (en) | 1992-04-02 | 2004-05-11 | Anticancer, Inc. | Method for promoting hair growth |
JP2950520B2 (ja) | 1993-04-02 | 1999-09-20 | アンティキャンサー インコーポレーテド | 毛胞に有益な配合物を送達する方法 |
CA2239976A1 (en) | 1995-09-20 | 1997-03-27 | Paul A. Zamecnik | Antisense oligonucleotide chemotherapy for benign hyperplasia or cancer of the prostate |
US6489163B1 (en) | 1996-05-08 | 2002-12-03 | Board Of Regents, The University Of Texas System | Ribozyme mediated inactivation of the androgen receptor |
EP1282699B1 (en) | 2000-05-04 | 2012-11-21 | Sarepta Therapeutics, Inc. | Splice-region antisense composition and method |
US20050159376A1 (en) * | 2002-02-20 | 2005-07-21 | Slrna Therapeutics, Inc. | RNA interference mediated inhibition 5-alpha reductase and androgen receptor gene expression using short interfering nucleic acid (siNA) |
JP4338527B2 (ja) * | 2002-04-05 | 2009-10-07 | サンタリス ファーマ アー/エス | HIF−1α発現を調節するオリゴマー化合物 |
US7087229B2 (en) | 2003-05-30 | 2006-08-08 | Enzon Pharmaceuticals, Inc. | Releasable polymeric conjugates based on aliphatic biodegradable linkers |
WO2004046160A2 (en) | 2002-11-18 | 2004-06-03 | Santaris Pharma A/S | Amino-lna, thio-lna and alpha-l-oxy-ln |
WO2004063331A2 (en) * | 2003-01-03 | 2004-07-29 | Gencia Corporation | SiRNA MEDIATED POST-TRANSRIPTIONAL GENE SILENCING OF GENES INVOLVED IN ALOPECIA |
CA2515554A1 (en) * | 2003-02-10 | 2004-08-19 | Santaris Pharma A/S | Oligomeric compounds for the modulation of thioredoxin expression |
EP1592795A2 (en) * | 2003-02-10 | 2005-11-09 | Santaris Pharma A/S | Oligomeric compounds for the modulation of ras expression |
AU2004230927B9 (en) | 2003-04-13 | 2011-12-01 | Enzon Pharmaceuticals, Inc. | Polymeric oligonucleotide prodrugs |
AU2004273828A1 (en) * | 2003-09-12 | 2005-03-31 | Avi Biopharma, Inc. | Compound and method for treating androgen-independent prostate cancer |
US20050164970A1 (en) | 2003-12-22 | 2005-07-28 | University Of Kansas Medical Center | Method for treating prostate cancer using siRNA duplex for androgen receptor |
JP4642775B2 (ja) * | 2003-12-23 | 2011-03-02 | サンタリス ファーマ アー/エス | Bcl−2のモデュレーションのためのオリゴマー化合物 |
WO2007031091A2 (en) | 2005-09-15 | 2007-03-22 | Santaris Pharma A/S | Rna antagonist compounds for the modulation of p21 ras expression |
AU2006291836B2 (en) | 2005-09-15 | 2012-02-23 | Santaris Pharma A/S | RNA antagonist compounds for the inhibition of Apo-Bl00 expression |
WO2007041497A2 (en) * | 2005-09-30 | 2007-04-12 | Cleveland Biolabs, Inc. | Modulation of androgen receptor |
EP2024503A2 (en) * | 2006-05-01 | 2009-02-18 | Aarhus Universitet | An animal model and a method for producing an animal model |
WO2007143315A2 (en) | 2006-05-05 | 2007-12-13 | Isis Pharmaceutical, Inc. | Compounds and methods for modulating expression of pcsk9 |
MX2009002859A (es) | 2006-09-15 | 2009-03-30 | Enzon Pharmaceuticals Inc | Enlazadores biodegradables a base de ester impedido para suministro de oligonucleotidos. |
JP2010503414A (ja) | 2006-09-15 | 2010-02-04 | エンゾン ファーマスーティカルズ インコーポレイテッド | 正に荷電した部分を含有するポリマー複合体 |
CN101554074B (zh) | 2006-10-30 | 2012-08-22 | 诺基亚公司 | 为用户设备提供运营商控制的移动性的方法、设备和系统 |
JP5168944B2 (ja) | 2007-02-28 | 2013-03-27 | 三浦工業株式会社 | 羽根車式流量計 |
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EA201070660A1 (ru) | 2010-12-30 |
CA2705714A1 (en) | 2009-06-04 |
JP2016105703A (ja) | 2016-06-16 |
DK2225377T3 (da) | 2014-04-07 |
EA020026B1 (ru) | 2014-08-29 |
WO2009068033A2 (en) | 2009-06-04 |
EP2225377B1 (en) | 2014-01-08 |
KR20100110298A (ko) | 2010-10-12 |
IL205944A (en) | 2015-11-30 |
IL222397A (en) | 2015-10-29 |
UA100253C2 (uk) | 2012-12-10 |
US7989429B2 (en) | 2011-08-02 |
NZ585327A (en) | 2012-10-26 |
MX2010005703A (es) | 2010-06-11 |
IL205944A0 (en) | 2010-11-30 |
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